Canonical Allele Identifier: CA10856143

Gene: IKBKE

Linked Data

• dbSNP Id: rs12142086
• gnomAD v2: 1-206657802-T-C
• gnomAD v3: 1-206484465-T-C
• gnomAD v4: 1-206484465-T-C
• MyVariant Identifiers: chr1:g.206657802T>C (hg19) ; chr1:g.206484465T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206484465T>C , CM000663.2:g.206484465T>C	GRCh38
NC_000001.10:g.206657802T>C , CM000663.1:g.206657802T>C	GRCh37
NC_000001.9:g.204724425T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000581977.7:c.1428-532T>C MANE Select	ENSP00000464030.1:n.1428-532T>C
ENST00000578328.6:c.1428-532T>C	ENSP00000473833.1:n.1428-532T>C
ENST00000581977.6:c.1428-532T>C	ENSP00000464030.1:n.1428-532T>C
ENST00000584998.5:c.1173-532T>C	ENSP00000462396.1:n.1173-532T>C
NM_001193321.1:c.1173-532T>C	NP_001180250.1:n.1173-532T>C
NM_001193322.1:c.1428-532T>C	NP_001180251.1:n.1428-532T>C
NM_014002.3:c.1428-532T>C	NP_054721.1:n.1428-532T>C
XM_005273356.2:c.1428-532T>C	XP_005273413.1:n.1428-532T>C
XR_922002.1:n.1802-532T>C
XM_017002868.1:c.1062-532T>C	XP_016858357.1:n.1062-532T>C
XR_922002.2:n.1780-532T>C
NM_014002.4:c.1428-532T>C MANE Select	NP_054721.1:n.1428-532T>C
NM_001193321.2:c.1173-532T>C	NP_001180250.1:n.1173-532T>C
NM_001193322.2:c.1428-532T>C	NP_001180251.1:n.1428-532T>C